Increasing Symptoms from a Bee Sting
Inquiry regarding my daughter My daughter, aged 13, weighs 85 pounds and stands at 5'2". She has no diagnosed medical conditions and does not take any medication. On Wednesday, she experienced a bee sting on the tip of her second toe. Initially, the swelling and redness subsided significantly by the following day, though some itching persisted. However, the situation appears to have worsened as the swelling has increased and the redness has spread beyond its original area. Should I be worried about this development, or is this a typical response to a bee sting? I wasn’t present at the time of the incident, so I’m uncertain about the type of bee involved.
Answers (1)

8/3/2025, 1:10:37 AM
OpenHealth AI
It’s understandable to be concerned about your daughter’s reaction to a bee sting, especially since it has worsened over time. While some swelling and redness can be typical after a bee sting, significant increases in swelling and redness that spreads could indicate a more severe reaction or infection.
Explanation: After a bee sting, it is common for the affected area to swell and become red as part of the body’s inflammatory response. However, if the swelling increases and redness spreads, this might suggest an allergic reaction or an infection at the sting site. Symptoms to look out for that indicate a more serious reaction include difficulty breathing, rapid swelling (especially of the face or throat), hives, or severe pain at the sting site.
Next Steps:
-
Monitor Symptoms: Keep a close eye on her symptoms. Check for any new symptoms such as fever, increasing pain, or additional swelling that extends beyond the immediate area of the sting.
-
Cold Compress: Apply a cold compress to the affected toe to help reduce swelling and discomfort. You can do this for 10-15 minutes at a time, several times a day.
-
Antihistamines: If the itching is bothersome, consider giving her an over-the-counter antihistamine (such as diphenhydramine or loratadine) to help alleviate it. Follow the dosing instructions provided on the packaging for her age and weight.
-
Keep the Area Clean: Gently clean the area with soap and water to reduce the risk of infection, and consider applying a topical antibiotic ointment if there are any broken skin areas.
-
Seek Care if Necessary: If her symptoms worsen, particularly if she develops significant swelling around her face or throat, difficulty breathing, or if the redness and swelling continues to spread rapidly, it’s important to seek medical attention promptly.
Monitoring the situation closely and taking these steps should help manage her symptoms effectively. If you're ever uncertain, or if she starts showing concerning signs, don't hesitate to seek further medical help.
Related Questions
Concern About Mild Cellulitis on Inner Thigh: Should I Be Worried?
At 30 years old, I've found myself facing what seems to be a mild case of cellulitis on the inner part of my thigh, and I can't help but feel unsettled about it. On Thursday evening, I noticed an unusual, dark purple pimple forming on the upper inner thigh. Unsurprisingly, I tried to pop it, but it was quite painful, and nothing came out. By Friday night, I observed that a red area, measuring around 1x2 inches, had developed around the blemish. Fast forward to Saturday afternoon, and the redness had intensified, expanding to about 2x3 inches. I sought medical attention at an urgent care clinic where a nurse practitioner drained the area and prescribed both oral and topical antibiotics, which I have been using diligently throughout the day. As of late Saturday, I'm uncertain if the size is still increasing, but the inflamed area appears to be morphing into a larger 3x3 blob; perhaps this is due to pulling off the bandage. My concern escalated when I browsed through Reddit and stumbled upon various accounts detailing severe cases of cellulitis. Horror stories filled the thread – tales of near-death experiences, unbearable pain, and even amputations. There seems to be a lack of reassurance, with most sharing tales of ineffective oral antibiotics that resulted in prolonged hospital stays on IVs rather than any comforting reports suggesting it would be okay. I am left wondering when I should seriously consider heading to the emergency room, especially since my symptoms seem limited to a light red oval surrounding the abscess. While I have dealt with skin infections before, this one is unusually alarming given its rapid growth. It's causing me quite a bit of anxiety, and it's interfering with my sleep.
Abdominal Discomfort and Concerns
Male, 29 years old, currently only taking 10mg of Ezetimibe for cholesterol management. As I approach the third week of experiencing discomfort in my abdomen, I've noticed a persistent sensation of pressure and bloating concentrated at the lower part of my torso. This feeling tends to change based on whether I am sitting or lying down. To articulate the experience, it resembles a bubble of air pushing upward beneath my ribs and extending into my lower back, as though air has detached from my internal organs and become lodged in my lower abdomen. I’ve sought medical attention at both an urgent care facility and from a specialist. My evaluations included a urine analysis, blood work, a breath test, and a CT scan both with and without contrast; however, these tests have yielded no clear findings. There are no obstructions, diverticulitis, infections, or swelling evident. The only notable result was a slight elevation in calcium levels from my blood tests, along with minor indications of fatty liver. I am currently waiting for an appointment with a gastroenterologist to schedule a colonoscopy, but I can’t shake the anxiety that this could indicate something more severe. Passing gas requires a small amount of effort, and defecation takes moderate effort. Nonetheless, it feels as if I am not fully evacuating my bowels. My stool is neither hard nor dark, nor is there any blood present. The only instance of loose stools occurred when I took a laxative under the impression that I was experiencing a blockage. My family medical history includes only my mother, who had uterine cancer. Are there any insights or advice?
Seeking Insight on Persistent Leg and Foot Issues
Hello Reddit community, I’m a 20-year-old female, standing at 5 feet 6 inches and weighing 130 pounds. For approximately five years, I have been experiencing numbness in my legs and feet. During my freshman year in high school, I participated in cross country and track without facing any problems. However, during my sophomore year, around 25 minutes into a run, I began noticing a peculiar numbness that starts at the lower part of my foot and spreads upwards along the back of my leg. Initially, this sensation would only occur late in my runs and would subside shortly after stopping. Over time, the onset of these symptoms has worsened, appearing sooner and lingering longer after activity. I've also dealt with noticeable weakness in my calf, ankle, and knee, which heightened my fear of potential falls while running cross country. After several sessions of physical therapy, I was sent to a cardiologist who suspected I might be suffering from popliteal artery entrapment syndrome (PAES). Following an ultrasound and angiogram conducted by local physicians, no issues were detected, leading to a referral for compartment testing to a specialist an hour away. This physician, after taking in my history and conducting several ultrasounds, expressed confidence in proceeding with a left leg medial approach for popliteal artery release, questioning the validity of prior tests. Regrettably, my recovery from surgery did not yield any improvement; my symptoms intensified and began to occur even when standing, not just during running as previously experienced. In pursuit of further answers, I approached the Mayo Clinic, where an extensive series of tests was conducted, but ultimately, I was left without a clear diagnosis. Now, I'm facing three treatment paths: a complete compartment release across all four areas to confirm or rule out the condition (which sounds overly invasive and risky), a more aggressive posterior popliteal entrapment procedure (though I wonder if previous surgery would have resolved PAES if it were the issue), or the option to receive Botox injections targeting both chronic exertional compartment syndrome (CECS) and PAES (this solution entails multiple injections for potentially temporary relief and may face insurance challenges). As a young, engaged nursing student, this situation is remarkably challenging. I struggle to stand for any substantial period without discomfort, leaving me feeling quite limited. I've encountered numerous physicians with differing opinions, making me feel somewhat lost in this situation. I would greatly appreciate any guidance or insight from those who might understand what I’m going through. At present, my symptoms include: - Numbness in my feet (distinct from the pins and needles sensation) after standing for around 30 minutes, walking briskly, or even running, which I rarely do now. - Pain behind my knees after standing for over half an hour, accompanied by discomfort and weakness in that area. - Weakness in my ankles, making it difficult to lift my foot while attempting to step forward. - General pain, weakness, and discomfort while standing or walking, with recovery taking several days. The following tests have been performed: - EMG (four instances, with one specifically to rule out tarsal tunnel syndrome) - MRI (five instances) - Lower Extremity Ultrasounds (six instances with popliteal entrapment maneuvers) - Compartment Testing (twice) - ECG/TEE - Blood Tests for Connective Tissue Disease - Evaluations for Dysautonomia, Autoimmunity/Paraneoplasia - Catecholamine Endocrine Study - Autonomic Reflex Screening - X-rays of the tibia and fibula - Angiograms (twice) - Exercise VO2 Max test - Overnight Oximetry monitor - Previous PAES release surgery Results from the Compartment Tests showed: Pre-exercise / Post-exercise readings: - Right Anterior: 14/27 - Right Lateral: 19/26 - Right Deep Posterior: 12/20 - Right Superficial Posterior: 12/21 - Left Anterior: 8/19 - Left Lateral: 20/29 - Left Deep Posterior: 12/14 - Left Superficial Posterior: 11/17 Thank you in advance for any support or insights you may be able to provide!
Changes in Vision: My Experience and Concerns
I'm a 22-year-old female weighing 210 pounds and residing in the U.S., and I have a mixed eye prescription. My journey with strabismus began with surgery at the age of two, followed by another procedure at fourteen. Unfortunately, the eye that was treated has started to become lazy again a few years post-surgery. Lately, it seems that my vision has deteriorated further, leading me to my latest prescription. I'm seeking clarity on what this indicates about my condition and what I might anticipate moving forward. Could it mean my eyesight will continue to decline? Right Eye (OD): Sphere +1.25, Cylinder -0.75 Left Eye (OS): Sphere -1.50, Cylinder -0.25
Could Suppressing My Immune System Alleviate Brain Fog?
I’m a 26-year-old male, standing at 5'10”, and I’m currently grappling with persistent brain fog and derealization that has haunted me for the past 15 years, alongside underlying depression stemming from these cognitive issues. I do not take any medication, consume alcohol approximately three times a week, and I neither smoke nor use recreational drugs. It all began 15 years ago when I contracted a viral infection, and since then, I have felt as if I'm trapped in a dream-like state, a sensation that is incredibly frustrating. Despite numerous medical evaluations, there isn’t any clear physical evidence pointing to the root cause of my symptoms. I occasionally receive diagnoses like atypical ADHD or Functional Neurological Disorder (FND), but they don’t fully capture my experience. While antidepressants can help with my low mood, they do little to alleviate the cloudiness in my thoughts. Since I strongly suspect that the virus I had triggered these ongoing issues, I am considering that either an ongoing infection or an exaggerated immune response could be at play. There is also a chance that antibodies might be targeting specific proteins, similar to those seen in Sjögren's syndrome. I’m contemplating whether intentionally suppressing my immune system could provide insights; it may help me determine if I feel better or worse by temporarily reducing immune activity. To achieve this, I think I could adopt a restrictive diet that limits A and B-complex vitamins, consume larger amounts of alcohol over several weeks, and minimize exposure to germs by spending more time at home. My goal would be to decrease antibody production significantly and monitor any changes in my symptoms. Of course, it’s crucial to distinguish the adverse effects of this approach from the normal sensations of brain fog. Feeling unwell and having a surreal experience are not synonymous. Ultimately, I am at a loss for solutions and deeply weary of living with these challenges day after day.